Water-mediated control of depolymerization step of glatiramer acetate synthesis

ABSTRACT

Methods of making copolymers are described.

This application claims priority to U.S. Provisional Application No. 61/166,608, filed Apr. 3, 2009 and U.S. Provisional Application No. 61/247,321, filed Sep. 30, 2009, both of which are hereby incorporated by reference.

BACKGROUND

Glatiramer acetate (also known as copolymer-1 and marketed as the active ingredient in COPAXONE® by Teva Pharmaceutical Industries Ltd., Israel) is used in the treatment of the relapsing-remitting form of multiple sclerosis (RRMS). According to the COPAXONE® product label, glatiramer acetate (GA) consists of the acetate salts of synthetic polypeptides containing four naturally occurring amino acids: L-glutamic acid, L-alanine, L-tyrosine, and L-lysine with a reported average molar fraction of 0.141, 0.427, 0.095, and 0.338, respectively. Chemically, glatiramer acetate is designated L-glutamic acid polymer with L-alanine, L-lysine and L-tyrosine, acetate (salt). Its structural formula is: (Glu,Ala,Lys,Tyr)_(x) ●xCH₃COOH (C₅H₉NO₄●C₃H₇NO₂●C₆H₁₄N₂O₂●C₉H₁₁NO₃)_(x) ●xC₂H₄O₂ CAS-147245-92-9

SUMMARY OF THE INVENTION

The invention is based, at least in part, on the identification of methods for controlling the level of L-pyroGlutamic Acid (pyro-Glu) in glatiramer acetate (GA). Pyro-Glu is present in GA, and the ability to control the level of pyro-Glu in GA is useful in controlling both product and process quality in the manufacture of GA.

Described herein is a method for preparing a composition comprising glatiramer acetate, comprising: polymerizing N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA) protected L-lysine and L-tyrosine to generate a protected copolymer (Intermediate-1); treating the protected copolymer to partially depolymerize the protected copolymer and deprotect benzyl protected groups thereby generating a partially depolymerized, benzyl-deprotected product (Intermediate-2); treating the partially depolymerized product to deprotect TFA-protected lysines thereby generating a TFA-deprotected product (Intermediate-3) and further processing the Intermediate-3 to create glatiramer acetate, wherein the improvement comprises: having water present during at least a portion of the depolymerization step.

Also described herein is a method for preparing a composition comprising glatiramer acetate, comprising: polymerizing N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA) protected L-lysine and L-tyrosine to generate a protected copolymer (Intermediate-1); treating the protected copolymer to partially depolymerize the protected copolymer and deprotect benzyl protected groups thereby generating a partially depolymerized, benzyl-deprotected product (Intermediate-2); and treating the partially depolymerized product to deprotect TFA-protected lysines thereby generating a TFA-deprotected product (Intermediate-3); and further processing the Intermediate-3 to create glatiramer acetate, wherein the improvement comprises: adjusting the water present during at least a portion of the depolymerization step so that amount water is present during at least a portion of the depolymerization step is within a predetermined range.

Also described herein is a method for preparing a composition comprising glatiramer acetate, comprising: polymerizing N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA) protected L-lysine and L-tyrosine to generate a protected copolymer (Intermediate-1); treating the protected copolymer to partially depolymerize the protected copolymer and deprotect benzyl protected groups thereby generating a partially depolymerized, benzyl-deprotected product (Intermediate-2); treating the partially depolymerized, benzyl-deprotected product to deprotect TFA-protected lysines thereby generating acetate TFA-deprotected product (Intermediate-3); and further processing Intermediate-3 to create glatiramer acetate, wherein the improvement comprises: controlling the water present during at least a portion of the depolymerization step so that amount water is present during at least a portion of the depolymerization step is within a predetermined range.

In various embodiments of the forgoing methods: water is present, adjusted or controlled at the beginning of the depolymerization step; water is added during the depolymerization step; the water present during the depolymerization step is present within a predetermined range (e.g., the predetermined range is 4-25%, 5-25%, 4-20%, 4-16%, 7-15%, 8-14%, 9-13%, 10-12%, 13-19%, 14-18% w/w against Intermediate-1); the depolymerization proceeds for 16-64 hrs, preferably at least 25 hrs (e.g., 25-55 hrs, at least 30 hrs, 30-50 hrs, at least 40 hrs, 43-47 hrs); the depolymerization reaction is carried out at 17-35° C., e.g., 18-30° C., 18-22° C.; the depolymerization step comprises contacting the protected copolymer with a solution comprising phenol, HBr and acetic acid; the concentration of pyroglu in the purified glatiramer acetate is 2000-7000 ppm (e.g., 2500-6000 ppm; 2500-5500 ppm; 3000-5000 ppm; 3500-4500 ppm, 2400-6500 ppm); the Mp of the purified glatiramer acetate is 5,000-9,000 Da (e.g., 6,500-7,500 Da); in one embodiment water is present during the depolymerization step at 11.2% w/w against Intermediate-1, the depolymerization proceeds for 43-47 hrs at 18-22° C. and the process produces purified glatiramer acetate in which pyro-Glu is present at 0.24-0.65% w/w (2400-6500 ppm). The improvement further comprises: preparing a pharmaceutical composition comprising at least a portion of the purified glatiramer acetate; and in some cases the method further includes measuring the amount of water in the depolymerization step at least once.

Also described is a method for preparing a composition comprising glatiramer acetate, comprising: polymerizing N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA) protected L-lysine and L-tyrosine to generate a protected copolymer; treating the protected copolymer to partially depolymerize the protected copolymer and deprotect benzyl protected groups thereby generating a partially depolymerized product; treating the partially depolymerized product to deprotect TFA-protected lysines thereby generating a TFA-deprotected product; and processing the TFA-deprotected product to create glatiramer acetate, wherein water is present during at least a portion of the depolymerization step.

An additional method is a method for preparing a composition comprising glatiramer acetate, comprising: polymerizing N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA) protected L-lysine and L-tyrosine to generate a protected copolymer; treating the protected copolymer to partially depolymerize the protected copolymer and deprotect benzyl protected groups thereby generating a partially depolymerized product; treating the partially depolymerized product to deprotect TFA-protected lysines thereby generating glatiramer acetate; and purifying the glatiramer acetate to create purified glatiramer acetate, wherein water is present during at least a portion of the depolymerization step within a predetermined range.

An additional described method is a method for preparing a composition comprising glatiramer acetate, comprising: polymerizing N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA) protected L-lysine and L-tyrosine to generate a protected copolymer; treating the protected copolymer to partially depolymerize the protected copolymer and deprotect benzyl protected groups thereby generating a partially depolymerized product; treating the partially depolymerized product to deprotect TFA-protected lysines thereby generating a TFA-deprotected product; and processing the a TFA-deprotected product; to create glatiramer acetate, wherein the water present during at least a portion of the depolymerization step is controlled to be within a predetermined range.

In various embodiments of the foregoing methods: water is present, adjusted or controlled at the beginning of the depolymerization step; water is added during the depolymerization step; the water present during the depolymerization step is present within a predetermined range (e.g., the predetermined range is 4-25%, 5-25%, 13-19%, 14-18% w/w against Intermediate-1); the depolymerization proceeds for at least 25 hrs (e.g., at least 30 hrs or at least 40 hrs); the depolymerization step comprises contacting the protected copolymer with a solution comprising phenol, HBr and acetic acid; the concentration of pyroglu in the purified glatiramer acetate is 2000-7000 ppm (e.g., 2500-6000 ppm; 2500-5500 ppm; 3000-5000 ppm; 3500-4500 ppm, 2400-6500 ppm (0.24%-0.65% w/w); the the Mp of the purified glatiramer acetate is 5,000-9,000 Da (e.g., 6,500-7,500 Da); the improvement further comprises: preparing a pharmaceutical composition comprising at least a portion of the purified glatiramer acetate; the step of treating the partially depolymerized product to deprotect TFA-protected lysines comprises treating the depolymerized product with piperidine; the protected copolymer is isolated and at least partially dried prior to treating the protected copolymer to partially depolymerize the protected copolymer and deprotect benzyl protected groups; the partially depolymerized product is isolated and at least partially dried prior to the step of treating the partially depolymerized product to deprotect TFA-protected lysines; in some cases the method further includes measuring the amount of water in the depolymerization step at least once.

As used herein, a “copolymer”, “amino acid copolymer” or “amino acid copolymer preparation” is a heterogeneous mixture of polypeptides comprising a defined plurality of different amino acids (typically between 2-10, e.g., between 3-6, different amino acids). A copolymer may be prepared from the polymerization of individual amino acids. The term “amino acid” is not limited to naturally occurring amino acids, but can include amino acid derivatives and/or amino acid analogs. For example, in an amino acid copolymer comprising tyrosine amino acids, one or more of the amino acids can be a homotyrosine. Further, an amino acid copolymer having one or more non-peptide or peptidomimetic bonds between two adjacent residues is included within this definition.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 depicts the structure of pyro-Glu.

FIG. 2 is a graph depicting the results of studies on the effect of the presence water in the depolymerization reaction used in glatiramer acetate production.

DETAILED DESCRIPTION OF THE INVENTION

Other than a statement about molecular weight and amino acid composition, which are recited in the FDA-approved label for the product, the label and other available literature for COPAXONE® does not provide detailed information about the physiochemical characteristics of the product. It has been previously found that Pyro-Glu (FIG. 1) is a component of Copaxone® (glatiramer acetate or GA) that is present within a predetermined range (U.S. Ser. No. 12/408,058). For example, in many cases the pyro-Glu content of a GA preparation can be between 2000 ppm and 7000 ppm or 2400-6500 ppm.

The production of GA entails polymerization of amino acids to produce a mixture of peptides, referred to as Intermediate-1, followed by partial depolymerization and deprotection of Intermediate-1 to yield Intermediate-2. It has now been found that the level of pyro-Glu in GA can be effectively controlled by controlling the water present during the depolymerization step of the GA manufacturing process, for example, by adjusting the water content at the beginning of and/or during the depolymerization step, e.g., by adding water to a predetermined level at the beginning or during the depolymerization step. Moreover, it has now been found that by properly controlling (e.g., adjusting) the amount of water present during the depolymerization step and the duration of the depolymerization step it is possible to produce GA with a specified pyro-Glu content and a specified peak molecular weight (Mp). In many cases it is specified to have the pyro-Glu content of copolymer or GA be 2000 to 7000 ppm, e.g., 2500-5500 ppm, e.g., 3000-5000 ppm, e.g., 3500-4500 ppm, 2400-6500 ppm, and the water present during the depolymerization reaction or added at the end of the depolymerization reaction is preferably controlled or adjusted to achieve this specified pyro-Glu content. In many cases it is desirable to have the peak molecular weight (Mp) of GA be 5,000 to 9,000 Da, e.g., 6,000 to 8,000 Da, as measured as described in U.S. Pat. No. 7,074,580.

Manufacture of Glatiramer Acetate

Generally, the process for the manufacture of glatiramer acetate includes the following steps:

-   -   Step 1: polymerization of N-carboxy anhydrides of L-alanine,         benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA)         protected L-lysine and L-tyrosine (collectively referred to as         NCAs) to result in a protected copolymer (Intermediate-1),     -   Step 2: depolymerization and benzyl deprotection of         Intermediate-1 using hydrobromic acid in acetic acid (e.g.,         phenol treated 33% HBr/acetic acid), and     -   Step 3: deprotection of the TFA-protected lysines on         Intermediate-2 (e.g., by treatment with piperdine) to create         Intermediate-3, followed by processing to generate GA and         further purification and drying of the isolated GA drug         substance.

In Step 1 of GA manufacture, the NCAs are co-polymerized in a predetermined ratio using diethylamine as an initiator. Upon consumption of the NCA components, the reaction mixture is quenched in water. The resulting protected polymer (Intermediate-1) is isolated and dried. In Step 2 of GA manufacture, Intermediate-1 is treated with phenol-treated 33% HBr in acetic acid (HBr/AcOH). This results in the cleavage of the benzyl protecting group on the glutamic acids as well as cleavage of peptide bonds throughout the polymer. After a period of time the reaction is quenched with water, and the product polymer is isolated by filtration and washed with water. The product polymer, Intermediate-2, has a reduced molecular weight relative to Intermediate-1. Intermediate-2 is dried before proceeding to Step 3. In Step 3, Intermediate-2 is treated with aqueous piperidine to remove the trifluoroacetyl group on the lysines. The resulting copolymer, Intermediate-3, is subsequently purified using diafiltration/ultrafiltration and the resulting acetate salt is dried to produce Glatiramer Acetate drug substance.

Methods for the manufacture of GA are described in the following publications: U.S. Pat. No. 3,849,550; WO 95/031990 and US 2007-0021324.

Control of pyro-Glu and Depolymerization with Water

As shown below, GA with a pyro-Glu content of about 4,000 ppm and a peak molecular weight (Mp) about 7,000 Da can prepared by having water present in the depolymerization reaction at about 16% w/w against Intermediate-1. While the amount of water present is expressed here relative to the amount Intermediate 1, the amount of water present can be expressed in any convenient manner, for example: w/w against the weight of Intermediate-1 added to the depolymerization reaction; w/w against the weight of phenol used to treat the HBr/acetic acid added to depolymerization reaction; w/w against the total weight of HBR/acetic acid added to depolymerization reaction; v/v against the total volume of HBr/acetic acid added to the depolymerization reaction; or w/w against the total weight of the depolymerization reaction. Thus, the amount of water present relative to HBr/AcOH on a v/v basis can be calculated from the amount of water present relative to Intermediate-1 on a w/w basis as follows: Vol_((water))/Vol_((HBR/AcOH))=(Wt_((water))/Wt_((Intermediate-1)))×(Wt_((Intermediate-1))/Wt_((HBr/AcOH)))×(Wt_((HBr/AcOH))/Vol_((HBr/AcOH)))×(Vol_((water))/Wt_((water)))=(Wt_((water))/Wt_((Intermediate-1)))×(Wt_((Intermediate-1))/Wt_((HBr/AcOH)))×(Density_((HBr/AcOH))/Density_((water)))

The water present during the depolymerization reaction can include water present in the Intermediate-1 added to the depolymerization reaction (e.g., by using Intermediate-1 that is not fully dried) and/or water that is added at the beginning or during the depolymerization reaction. Thus, the amount of water present during at least a portion of the depolymerization reaction can be controlled by adding water to the reaction to achieve a predetermined level of water or by having a certain amount of water present in the Intermediate-1 added to the reaction or by a combination of adding water and having water present in the Intermediate-1. Thus, the amount of water present can be controlled by simply having a reasonably consistent amount of water present in the Intermediate-1. Water can be added to the depolymerization reaction at any time, but is most often present at a predetermined level, e.g., 4-25%, 5-25%, 10-20%, 4-20%, 4-16%, 7-15%, 8-14%, 9-13%, 10-12%, 13-19%, 14-18%, 15-17%, or 16% w/w against the weight of Intermediate-1, at the beginning of the depolymerization reaction. Because the depolymerization reaction can both consume and produce water, the amount of water present can change slightly over the course of the depolymerization reaction.

The amount of water present during the depolymerization step can impact the pyro-Glu content and molecular weight of the resulting GA, as shown by the experiments described below. However, the amount of water present during the depolymerization step can vary over a reasonable range and still be compatible with the production of GA having a desirable pyro-Glu content and molecular weight.

EXAMPLES Example 1

The effect of water present during the depolymerization step, Step 2, on the pyro-Glu content and molecular weight of the resulting GA was examined as follows. Intermediate-1 was produced as described above and divided between two depolymerization reactions (A and B). For Depolymerization reaction A, no water was added. For Depolymerization reaction B, water was added to 16% measured w/w against Intermediate-1. Depolymerization was allowed to proceed at 20° C. Aliquots removed periodically from each reaction were quenched with water and further processed to produce GA. The pyro-Glu content (ppm), measured as described below, and peak molecular weight (Mp) of each of the resulting GA samples were measured. The results of this analysis are shown in FIG. 2. The molecular weight (Mp) scale (Da) is on the left axis, the pyro-Glu concentration scale (ppm) is on the right axis. The time of Depolymerization reaction A (no added water) is on the upper horizontal axis, and the time of Depolymerization reaction B (water present at 16% w/w against intermediate-1) is on the lower horizontal axis. The scale of the graph is such that the horizontal line labeled “Midpoint of desired range of GPC-Mp (Da)/Midpoint of the desired range of pyroGlu (ppm)” indicates both one desirable Mp molecular weight (7,000 Da) and one desirable pyro-Glu concentration for GA (4,000 ppm). The lines labeled MW_(A) and MW_(B) depict the Mp molecular weight of the GA produced from material removed from Depolymerization reaction A and Depolymerization reaction B, respectively, at various time points. The lines labeled Py_(A) and Py_(B) depict the concentration pyro-Glu in the GA produced from material removed from Depolymerization reaction A and Depolymerization reaction B, respectively, at various time points.

In the absence of added water, the desired combination of molecular weight and pyro-Glu concentration is not achieved. As can be seen in FIG. 2, after about 12 hours (scale on upper horizontal axis) Depolymerization reaction A (no added water) produces material that yields GA having a desired pyro-Glu concentration (about 4,000 ppm), but the molecular weight (Mp) of the GA is about 7,400 Da, above the desired 7,000 Da. As can be also seen in FIG. 2, after about 26 hours (scale on upper horizontal axis) Depolymerization reaction A (no added water) produces material that yields GA having a desired Mp (about 7,000 Da), but the pyro-Glu concentration of the GA is greater than 6,000 ppm, which is above 4,000 ppm (the midpoint of the desired range). In contrast, when water is added to the depolymerization reaction to 16% (w/w against Intermediate-1), the desired combination of molecular weight and pyro-Glu concentration is achieved. As can also be seen from FIG. 2, after about 43 hours Depolymerization reaction B (16% water w/w against Intermediate-1) produces material that yields GA having a desired molecular weight (Mp about 7,000 Da) and a desired pyro-Glu concentration (about 4,000 ppm).

Example 2

In the study described above pyro-Glu concentration of GA was measured as follows. N-terminal pyro-Glu residues were cleaved using Pyrococcus furiosus pyro-glutamate aminopeptidase. Pyro-Glu in the resulting enzymatic hydrolysate is isolated by reverse phase liquid chromatography followed by detection at 200 nm using a reference standard curve prepared with known concentrations of L-Pyro-glutamate. Neurotensin (a commercially available polypeptide having 100% pyro-glutamate at the N-terminus) is assayed as a control to ensure the acceptability of the digestion and adequacy of the HPLC separation. The chromatographic analysis is performed using a Waters Atlantis C18 HPLC column and an isocratic mobile phase consisting of 100% Water, adjusted to pH 2.1 with phosphoric acid. Samples and Standards are held at 2-8° C. The peak corresponding to the pyro-glutamate moiety elutes at a retention time of approximately 12 minutes. The direct measure of pyro-glutamate content is on a w/w basis and the results are expressed as ppm (microgram/gram). 

What is claimed is:
 1. A method for preparing a composition comprising purified glatiramer acetate having a pyro-Glu concentration of 2000-7000 ppm and a Mp of 5000-9000 Da, comprising: polymerizing N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA) protected L-lysine and L-tyrosine to generate a protected copolymer (Intermediate-1); treating the protected copolymer with HBr and acetic acid to partially depolymerize the protected copolymer and deprotect benzyl protected groups thereby generating a partially depolymerized product; treating the partially depolymerized product with piperidine to deprotect TFA-protected lysines thereby generating glatiramer acetate; and purifying the glatiramer acetate to create purified glatiramer acetate having a pyro-Glu concentration of 2000-7000 ppm and a Mp of 5000-9000 Da, wherein water is present during the entirety of the depolymerization step in an amount that yields glatiramer acetate having a pyro-Glu concentration of 2000-7000 ppm and a Mp of 5000-9000 Da.
 2. A method for preparing a composition comprising purified glatiramer acetate having a pyro-Glu concentration of 2000-7000 ppm and a Mp of 5000-9000 Da, comprising: polymerizing N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA) protected L-lysine and L-tyrosine to generate a protected copolymer (Intermediate-1); treating the protected copolymer with HBr and acetic acid to partially depolymerize the protected copolymer and deprotect benzyl protected groups thereby generating a partially depolymerized product; treating the partially depolymerized product with piperidine to deprotect TFA-protected lysines thereby generating glatiramer acetate; and purifying the glatiramer acetate to create purified glatiramer acetate having a pyro-Glu concentration of 2000-7000 ppm and a Mp of 5000-9000 Da, wherein the amount of water present during the entirety of the depolymerization step is adjusted to be within a predetermined range that yields glatiramer acetate having a pyroglutamate concentration of 2000-7000 ppm and a Mp of 5000-9000 Da.
 3. A method for preparing a composition comprising purified glatiramer acetate having a pyroglutamate concentration of 2000-7000 ppm and a Mp of 5000-9000 Da, comprising: polymerizing N-carboxy anhydrides of L-alanine, benzyl-protected L-glutamic acid, trifluoroacetic acid (TFA) protected L-lysine and L-tyrosine to generate a protected copolymer (Intermediate-1); treating the protected copolymer with HBr and acetic acid to partially depolymerize the protected copolymer and deprotect benzyl protected groups thereby generating a partially depolymerized product; treating the partially depolymerized product with piperidine to deprotect TFA-protected lysines thereby generating glatiramer acetate; and purifying the glatiramer acetate to create purified glatiramer acetate having a pyro-Glu concentration of 2000-7000 ppm and a Mp of 5000-9000 Da, wherein the amount of water present during the entirety of the depolymerization step is controlled to be within a predetermined range that yields glatiramer acetate having a pyro-Glu concentration of 2000-7000 ppm and a Mp of 5000-9000 Da.
 4. The method of any one of claims 1, 2, and 3, wherein water is added during the depolymerization step.
 5. The method of claim 1, wherein the amount of water present during the depolymerization step is within a predetermined range.
 6. The method of claim 2, wherein the predetermined range is 4-25% w/w against Intermediate-1 present at the beginning of the depolymerization reaction.
 7. The method of claim 2, wherein the predetermined range is 13-19% w/w against Intermediate-1 present at the beginning of the depolymerization reaction.
 8. The method of claim 2, wherein the predetermined range is 14-18% w/w against Intermediate-1 present at the beginning of the depolymerization reaction.
 9. The method of claim 1, wherein the depolymerization proceeds for at least 25 hrs.
 10. The method of claim 9, wherein the depolymerization proceeds for at least 30 hrs.
 11. The method of claim 10, wherein the depolymerization proceeds for at least 40 hrs.
 12. The method of claim 1, wherein the depolymerization step comprises contacting the protected copolymer with a solution comprising phenol, HBr and acetic acid.
 13. The method of claim 1, wherein the concentration of pyro-Glu in the purified glatiramer acetate is 2500-5500 ppm.
 14. The method of claim 1, wherein the concentration of pyro-Glu in the purified glatiramer acetate is 3000-5000 ppm.
 15. The method of claim 1, wherein the concentration of gyro-Glu in the purified glatiramer acetate is 3500-4500 ppm.
 16. The method of any one of claims 1, 13, 14 and 15, wherein the Mp of the purified glatiramer acetate is 6,500-7,500 Da.
 17. The method of claim 1, wherein the protected copolymer is isolated and at least partially dried prior to treating the protected copolymer to partially depolymerize the protected copolymer and deprotect benzyl protected groups.
 18. The method of claim 1, wherein the partially depolymerized product is isolated and at least partially dried prior to the step of treating the partially depolymerized product to deprotect TFA-protected lysines.
 19. The method of claim 1, further comprising measuring the amount of water in the depolymerization step at least once.
 20. The method of claim 1, further comprising: preparing a pharmaceutical composition comprising at least a portion of the purified glatiramer acetate.
 21. The method of claim 5, wherein the predetermined range is 4-25% w/w against Intermediate-1 present at the beginning of the depolymerization reaction.
 22. The method of claim 21, wherein the predetermined range is 13-19% w/w against Intermediate-1 present at the beginning of the depolymerization reaction.
 23. The method of claim 22, wherein the predetermined range is 14-18% w/w against Intermediate-1 present at the beginning of the depolymerization reaction.
 24. The method of claim 3, wherein the predetermined range is 4-25% w/w against Intermediate-1 present at the beginning of the depolymerization reaction.
 25. The method of claim 24, wherein the predetermined range is 13-19% w/w against Intermediate-1 present at the beginning of the depolymerization reaction.
 26. The method of claim 25, wherein the predetermined range is 14-18% w/w against Intermediate-1 present at the beginning of the depolymerization reaction.
 27. The method of claim 2, wherein the depolymerization proceeds for at least 25 hrs.
 28. The method of claim 27, wherein the depolymerization proceeds for at least 30 hrs.
 29. The method of claim 28, wherein the depolymerization proceeds for at least 40 hrs.
 30. The method of claim 2, wherein the depolymerization step comprises contacting the protected copolymer with a solution comprising phenol, HBr and acetic acid.
 31. The method of claim 2, wherein the concentration of pyro-Glu in the purified glatiramer acetate is 2500-5500 ppm.
 32. The method of claim 31, wherein the concentration of pyro-Glu in the purified glatiramer acetate is 3000-5000 ppm.
 33. The method of claim 32, wherein the concentration of pyro-Glu in the purified glatiramer acetate is 3500-4500 ppm.
 34. The method of any one of claims 2, 31, 32, and 33, wherein the Mp of the purified glatiramer acetate is 6,500-7,500 Da.
 35. The method of claim 2, further comprising preparing a pharmaceutical composition comprising at least a portion of the purified glatiramer acetate.
 36. The method of claim 3, wherein the depolymerization proceeds for at least 25 hrs.
 37. The method of claim 36, wherein the depolymerization proceeds for at least 30 hrs.
 38. The method of claim 37, wherein the depolymerization proceeds for at least 40 hrs.
 39. The method of claim 3, wherein the concentration of pyro-Glu in the purified glatiramer acetate is 2500-5500 ppm.
 40. The method of claim 39, wherein the concentration of pyro-Glu in the purified glatiramer acetate is 3000-5000 ppm.
 41. The method of claim 40, wherein the concentration of pyro-Glu in the purified glatiramer acetate is 3500-4500 ppm.
 42. The method of any one of claims 3, 39, 40 and 41, wherein the Mp of the purified glatiramer acetate is 6,500-7,500 Da.
 43. The method of claim 3 further comprising preparing a pharmaceutical composition comprising at least a portion of the purified glatiramer acetate.
 44. The method of claim 3, wherein the depolymerization step comprises contacting the protected copolymer with a solution comprising phenol, HBr and acetic acid.
 45. The method of claim 2, wherein the protected copolymer is isolated and at least partially dried prior to treating the protected copolymer to partially depolymerize the protected copolymer and deprotect benzyl protected groups.
 46. The method of claim 2, wherein the partially depolymerized product is isolated and at least partially dried prior to the step of treating the partially depolymerized product to deprotect TFA-protected lysines.
 47. The method of claim 2, further comprising measuring the amount of water in the depolymerization step at least once.
 48. The method of claim 3, wherein the protected copolymer is isolated and at least partially dried prior to treating the protected copolymer to partially depolymerize the protected copolymer and deprotect benzyl protected groups.
 49. The method of claim 3, wherein the partially depolymerized product is isolated and at least partially dried prior to the step of treating the partially depolymerized product to deprotect TFA-protected lysines.
 50. The method of claim 3, further comprising measuring the amount of water in the depolymerization step at least once.
 51. The method of any of claims 2, 3 and 5 wherein water is added at the beginning of the depolymerization step.
 52. The method of claim 51, wherein water is added at the beginning of the depolymerization step to be within the predetermined range of 4-25% w/w against Intermediate-11 present at the beginning of the depolymerization reaction.
 53. The method of claim 51, wherein water is added at the beginning of the depolymerization step to be within the predetermined range of 13-19% w/w against Intermediate-1 present at the beginning of the depolymerization reaction.
 54. The method of claim 51, wherein water is added at the beginning of the depolymerization step to be within the predetermined range of 14-18% w/w against Intermediate-1 present at the beginning of the depolymerization reaction.
 55. The method of claim 1 wherein water is present at 4-25% w/w against Intermediate-1 present at the beginning of the depolymerization reaction.
 56. The method of claim 1 wherein water is present at 13-19% w/w against Intermediate-1 present at the beginning of the depolymerization reaction.
 57. The method of claim 1 wherein water is present at 14-18% w/w against Intermediate-1 present at the beginning of the depolymerization reaction. 